|
Symbol Name ID |
Rgr
retinal G protein coupled receptor MGI:1929473 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc pallor |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Rod-cone dystrophy |
Abnormal electroretinogram |
Decreased light- and dark-adapted electroretinogram amplitude |
Nystagmus |
Ophthalmoplegia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Constriction of peripheral visual field |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with RGR | |||||||||||||||||||||||
| retinitis pigmentosa | |||||||||||||||||||||||
| retinitis pigmentosa 44 |
| Mouse Phenotypes | abnormal eye physiology |
abnormal eye electrophysiology |
|
| Availability | Mouse Genotype | ||
| Rgrtm1Hkf/Rgrtm1Hkf | |||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools